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. 2005 Jun 17;37(6):386–390. doi: 10.1111/j.1745-7270.2005.00058.x

Dose‐dependent Inhibition of Gynecophoral Canal Protein Gene Expression in Vitro in the Schistosome (Schistosoma japonicum) by RNA Interference

Guo‐Feng CHENG 1, Jiao‐Jiao LIN 1, Yi SHI 2, You‐Xin JIN 2,, Zhi‐Qiang FU 1, Ya‐Mei JIN 1, Yuan‐Cong ZHOU 2, You‐Min CAI 1,
PMCID: PMC7185640  PMID: 15944753

Abstract

Abstract The gynecophoral canal protein gene SjGCP of Schistosoma japonicum that is necessary for the pairing between the male and female worms is specifically expressed in the adult male worm. This protein is widely distributed in the adult female worm after pairing. Reverse transcription‐polymerase chain reaction (RT‐PCR) and immunofluorescence were employed to analyze the relationship between the RNAi effect and dsRNA dosage in the parasites. The results revealed that the inhibition of SjGCP expression by siRNA is dose‐dependent. RT‐PCR analysis showed that the SjGCP transcript level was reduced by 75% when 100 nM dsRNA was applied.

Edited by: Wang‐Yi LIU

Keywords: RNA interference, gynecophoral canal protein gene, Schistosoma japonicum, dosage

This work was supported by the grants from the Shanghai Important Science and Technology Key Program of China (No. 03DZ19231), the Shanghai Program for Phosphor Plan of China (No. 04QMX1462) and the National Natural Science Foundation of China (No. 30270311)

References

  • 1. Chen XY, Jiang QW, Wang LY, Zhao GM, Zhao Q, Gu GA, Wei JG et al. Schistosomasis situation in the People's Republic of China in 2001. Chin J Schisto Control 2002, 14: 241–243. [Google Scholar]
  • 2. Erasmus DA. A comparative study of the reproductive system of mature, immature and “unisexual” female Schistosoma mansoni. Parasitology 1973, 67: 165–183. [DOI] [PubMed] [Google Scholar]
  • 3. Basch PF. Schistosoma mansoni: Nucleic acid synthesis in immature females from single‐sex infections, paired in vitro with intact males and male segments. Comp Biochem Physiol B 1988, 90: 389–392. [DOI] [PubMed] [Google Scholar]
  • 4. Cheng GF, Lin JJ, Feng XG, Fu ZQ, Jin YM, Yuan CX, Zhou YC et al. Proteomic analysis of differentially expressed proteins between male and female worm of Schistosoma japonicum after pairing. Proteomics 2005, 5: 511–521. [DOI] [PubMed] [Google Scholar]
  • 5. den Hollander JE, Erasmus DA. Schistosoma mansoni: Male stimulation and DNA synthesis by the female. Parasitology 1985, 91: 449–457. [DOI] [PubMed] [Google Scholar]
  • 6. Gupta BC, Basch PF. The role of Schistosoma mansoni males in feeding and development of female worms. J Parasitol 1987, 73: 481–486. [PubMed] [Google Scholar]
  • 7. LoVerde PT, Chen L. Schistosome female reproductive development. Parasitol Today 1991, 7: 303–308. [DOI] [PubMed] [Google Scholar]
  • 8. LoVerde PT, Niles EG, Osman A, Wu W. Schistosoma mansoni: Male‐female interactions. Can J Zool 2004, 82: 357–374. [Google Scholar]
  • 9. Chen LL, Rekosh DM, LoVerde PT. Schistosoma mansoni p48 eggshell protein gene: Characterization, developmentally regulated expression and comparison to the p14 eggshell protein gene. Mol Biochem Parasitol 1992, 52: 39–52. [DOI] [PubMed] [Google Scholar]
  • 10. Grevelding CG, Sommer G, Kunz W. Female‐specific gene expression in Schistosoma mansoni is regulated by pairing. Parasitology 1997, 115: 635–640. [DOI] [PubMed] [Google Scholar]
  • 11. LoVerde PT, Rekosh DM, Bobek LA. Developmentally regulated gene expression in Schistosoma. Exp Parasitol 1989, 68: 116–120. [DOI] [PubMed] [Google Scholar]
  • 12. Menrath M, Michel A, Kunz W. A female‐specific cDNA sequence of Schistosoma mansoni encoding a mucin‐like protein that is expressed in the epithelial cells of the reproductive duct. Parasitology 1995, 111: 477–483. [DOI] [PubMed] [Google Scholar]
  • 13. Schussler P, Grevelding CG, Kunz W. Identification of Ras, MAP kinases, and a GAP protein in Schistosoma mansoni by immunoblotting and their putative involvement in male–female interaction. Parasitology 1997, 115: 629–634. [DOI] [PubMed] [Google Scholar]
  • 14. Siegel DA, Tracy JW. Schistosoma mansoni: Influence of the female parasite on glutathione biosynthesis in the male. Exp Parasitol 1989, 69: 116–124. [DOI] [PubMed] [Google Scholar]
  • 15. Bostic JR, Strand M. Molecular cloning of a Schistosoma mansoni protein expressed in the gynecophoral canal of male worms. Mol Biochem Parasitol 1996, 79: 79–89. [DOI] [PubMed] [Google Scholar]
  • 16. Elbashir SM, Harborth J, Weber K, Tuschl T. Analysis of gene function in somatic mammalian cells using small interfering RNAs. Methods 2002, 26: 199–213. [DOI] [PubMed] [Google Scholar]
  • 17. Fire A, Xu S, Montgomery MK, Kostas SA, Driver SE, Mello CC. Potent and specific genetic interference by double‐stranded RNA in Caenorhabditis elegans. Nature 1998, 391: 806–811. [DOI] [PubMed] [Google Scholar]
  • 18. Kamath RS, Martinez‐Campos M, Zipperlen P, Fraser AG, Ahringer J. Effectiveness of specific RNA‐mediated interference through ingested double‐stranded RNA in Caenorhabditis elegans. Genome Biol 2001, 2: RESEARCH0002. [DOI] [PMC free article] [PubMed] [Google Scholar]

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